Immortalized Human Dorsal Root Ganglion Cells Differentiate into Neurons with Nociceptive Properties

A renewable source of human sensory neurons would greatly facilitate basic research and drug development. We had established previously conditionally immortalized human CNS cell lines that can differentiate into functional neurons (). We report here the development of an immortalized human dorsal ro...

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Veröffentlicht in:The Journal of neuroscience 1999-07, Vol.19 (13), p.5420-5428
Hauptverfasser: Raymon, Heather K, Thode, Silke, Zhou, Jiuying, Friedman, Glenn C, Pardinas, Jose R, Barrere, Christian, Johnson, Randolph M, Sah, Dinah W. Y
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container_end_page 5428
container_issue 13
container_start_page 5420
container_title The Journal of neuroscience
container_volume 19
creator Raymon, Heather K
Thode, Silke
Zhou, Jiuying
Friedman, Glenn C
Pardinas, Jose R
Barrere, Christian
Johnson, Randolph M
Sah, Dinah W. Y
description A renewable source of human sensory neurons would greatly facilitate basic research and drug development. We had established previously conditionally immortalized human CNS cell lines that can differentiate into functional neurons (). We report here the development of an immortalized human dorsal root ganglion (DRG) clonal cell line, HD10.6, with a tetracycline-regulatable v-myc oncogene. In the proliferative condition, HD10.6 cells have a doubling time of 1.2 d and exhibit a neuronal precursor morphology. After differentiation of clone HD10.6 for 7 d in the presence of tetracycline, v-myc expression was suppressed, and >50% of the cells exhibited typical neuronal morphology, stained positively for neuronal cytoskeletal markers, and fired action potentials in response to current injection. Furthermore, this cell line was fate-restricted to a neuronal phenotype; even in culture conditions that promote Schwann cell or smooth muscle differentiation of neural crest stem cells, HD10.6 differentiated exclusively into neurons. Moreover, differentiated HD10.6 cells expressed sensory neuron-associated transcription factors and exhibited capsaicin sensitivity. Taken together, these data indicate that we have established an immortalized human DRG cell line that can differentiate into sensory neurons with nociceptive properties. The cell line HD10.6 represents the first example of a human sensory neuronal line and will be valuable for basic research, as well as for the discovery of novel drug targets and clinical candidates.
doi_str_mv 10.1523/jneurosci.19-13-05420.1999
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We had established previously conditionally immortalized human CNS cell lines that can differentiate into functional neurons (). We report here the development of an immortalized human dorsal root ganglion (DRG) clonal cell line, HD10.6, with a tetracycline-regulatable v-myc oncogene. In the proliferative condition, HD10.6 cells have a doubling time of 1.2 d and exhibit a neuronal precursor morphology. After differentiation of clone HD10.6 for 7 d in the presence of tetracycline, v-myc expression was suppressed, and &gt;50% of the cells exhibited typical neuronal morphology, stained positively for neuronal cytoskeletal markers, and fired action potentials in response to current injection. Furthermore, this cell line was fate-restricted to a neuronal phenotype; even in culture conditions that promote Schwann cell or smooth muscle differentiation of neural crest stem cells, HD10.6 differentiated exclusively into neurons. Moreover, differentiated HD10.6 cells expressed sensory neuron-associated transcription factors and exhibited capsaicin sensitivity. Taken together, these data indicate that we have established an immortalized human DRG cell line that can differentiate into sensory neurons with nociceptive properties. 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subjects Action Potentials
Capsaicin - pharmacology
Cations - metabolism
Cell Differentiation
Cell Line
Cell Lineage
Cell Size
Clone Cells - cytology
Clone Cells - drug effects
Clone Cells - metabolism
Ganglia, Spinal - cytology
Ganglia, Spinal - embryology
Genes, myc - genetics
Humans
Ion Channel Gating
Ligands
Neurons, Afferent - cytology
Neurons, Afferent - drug effects
Neurons, Afferent - metabolism
Neurons, Afferent - physiology
Nociceptors - physiology
Pain
Stem Cells - cytology
Stem Cells - drug effects
Stem Cells - metabolism
Tetracycline - pharmacology
Transcription Factors - analysis
title Immortalized Human Dorsal Root Ganglion Cells Differentiate into Neurons with Nociceptive Properties
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